» Articles » PMID: 30558868

Regional Gray Matter Changes and Age Predict Individual Treatment Response in Parkinson's Disease

Overview
Journal Neuroimage Clin
Publisher Elsevier
Specialties Neurology
Radiology
Date 2018 Dec 19
PMID 30558868
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

We aimed at testing the potential of biomarkers in predicting individual patient response to dopaminergic therapy for Parkinson's disease. Treatment efficacy was assessed in 30 Parkinson's disease patients as motor symptoms improvement from unmedicated to medicated state as assessed by the Unified Parkinson's Disease Rating Scale score III. Patients were stratified into weak and strong responders according to the individual treatment response. A multiple regression was implemented to test the prediction accuracy of age, disease duration and treatment dose and length. Univariate voxel-based morphometry was applied to investigate differences between the two groups on age-corrected T1-weighted magnetic resonance images. Multivariate support vector machine classification was used to predict individual treatment response based on neuroimaging data. Among clinical data, increasing age predicted a weaker treatment response. Additionally, weak responders presented greater brain atrophy in the left temporoparietal operculum. Support vector machine classification revealed that gray matter density in this brain region, including additionally the supplementary and primary motor areas and the cerebellum, was able to differentiate weak and strong responders with 74% accuracy. Remarkably, age and regional gray matter density of the left temporoparietal operculum predicted both and independently treatment response as shown in a combined regression analysis. In conclusion, both increasing age and reduced gray matter density are valid and independent predictors of dopaminergic therapy response in Parkinson's disease.

Citing Articles

Houston, We Have AI Problem! Quality Issues with Neuroimaging-Based Artificial Intelligence in Parkinson's Disease: A Systematic Review.

Dzialas V, Doering E, Eich H, Strafella A, Vaillancourt D, Simonyan K Mov Disord. 2024; 39(12):2130-2143.

PMID: 39235364 PMC: 11657025. DOI: 10.1002/mds.30002.


Unlocking the potential: T1-weighed MRI as a powerful predictor of levodopa response in Parkinson's disease.

Yan J, Luo X, Xu J, Li D, Qiu L, Li D Insights Imaging. 2024; 15(1):141.

PMID: 38853208 PMC: 11162980. DOI: 10.1186/s13244-024-01690-z.


Voxel-based morphometry of grey matter structures in Parkinson's Disease with wearing-off.

Zhai H, Fan W, Xiao Y, Zhu Z, Ding Y, He C Brain Imaging Behav. 2023; 17(6):725-737.

PMID: 37735325 PMC: 10733201. DOI: 10.1007/s11682-023-00793-3.


Hybrid CNN-LSTM model with efficient hyperparameter tuning for prediction of Parkinson's disease.

Lilhore U, Dalal S, Faujdar N, Margala M, Chakrabarti P, Chakrabarti T Sci Rep. 2023; 13(1):14605.

PMID: 37669970 PMC: 10480168. DOI: 10.1038/s41598-023-41314-y.


Surface-based morphological patterns associated with neuropsychological performance, symptom severity, and treatment response in Parkinson's disease.

Mo J, Yang B, Wang X, Zhang J, Hu W, Zhang C Ann Transl Med. 2022; 10(13):741.

PMID: 35957730 PMC: 9358503. DOI: 10.21037/atm-22-630.